BIOTOP PROFESSIONAL ANTISEPTIC HAND SANITIZER

Manufacturer
G.V. COSMETICS LTD
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:42

Label at a glance#

ProductBIOTOP PROFESSIONAL ANTISEPTIC HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product  to avoid swallowing

Storage and handling

store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children under 6 years of age when using this product to avoid swallowing

Other information 

STORAGE AND HANDLING SECTION

  • store between 15-30°C (59-86°F)
  • avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, aloe vera (Aloe barbadensis) leaf water, alpha-isomethyl ionone, benzalkonium chloride, benzyl alcohol, butylphenyl methylpropional, FD&C Blue No. 1, fragrance, glycerin, potassium sorbate, sodium benzoate, triethanolamine, water

SPL UNCLASSIFIED SECTION

Rinse- free | with Aloe Vera

Manufactured by: G.V. Cosmetics Ltd.
34 Ben-Zion Galis St. Segula,Petach Tikva, Israel, 4927934

Made In Israel

You may also report serious side effects to this address.
BIOTOP PROFESSIONAL USA, INC.
2723 W Touhy Ave, Chicago, IL 60645

www.biotopworld.com | Info@biotopworld.com

Lot No:
Expiry:

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79096-00179096-001-60, 79096-001-10, 79096-001-33, 79096-001-50, 79096-001-51

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
af15fcff-f0d7-49d8-8755-640af6c779b4019458e2-6231-44eb-af39-a06f0367bd7f2023-12-05WarningsExact identifier
spl set id: 019458e2-6231-44eb-af39-a06f0367bd7f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.